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Valence states of transition-metal ions in cubic perovskites SrMn1-xFexO3

Authors
Lee HJ (Lee, H. J.)Kim G (Kim, G.)Kang JS (Kang, J.-S.)Dabrowski B (Dabrowski, B.)Han SW (Han, S. W.)Lee SS (Lee, S. S.)Hwang C (Hwang, C.)Jung MC (Jung, M. C.)Shin HJ (Shin, H. J.)Lee HG (Lee, H. G.)Kim JY (Kim, J.-Y.)Min BI (Min, B. I.)
Issue Date
May-2007
Publisher
AMER INST PHYSICS
Citation
JOURNAL OF APPLIED PHYSICS, v.101, no.9, pp 1 - 3
Pages
3
Journal Title
JOURNAL OF APPLIED PHYSICS
Volume
101
Number
9
Start Page
1
End Page
3
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/148428
DOI
10.1063/1.2713206
ISSN
0021-8979
1089-7550
Abstract
The electronic structures of SrMn1-xFexO3 (0 <= x <= 1) have been investigated by using photoemission spectroscopy (PES) and soft x-ray absorption spectroscopy (XAS). Mn ions in SrMnO3 are found to be in the nearly tetravalent (Mn4+) states, but with a small mixture of the Mn2+ configuration. With increasing x in SrMn1-xFexO3, Mn ions remain in the 4+ states. Fe ions in SrMn1-xFexO3 are also in the nearly tetravalent (Fe4+) states for the whole range of x. Valence-band PES reveals that the occupied Mn t(2g)(3) states are located about 2.5 eV below E-F, while the occupied Fe t(2g)(3)e(g)(1) states are broader than the Mn 3d occupied states, and are located between 3 and 6 eV below E-F. The large overlap between Fe 3d and the O 2p states is found in SrFeO3, reflecting the strong hybridization between the Fe 3d states and the O 2p states, in agreement with the metallic nature of SrFeO3. (c) 2007 American Institute of Physics.
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